scholarly journals Decreased expression of Annexin A10 in gastric cancer and its overexpression in tumor cell growth suppression

2010 ◽  
Vol 24 (3) ◽  
Author(s):  
Nam
Keyword(s):  
Gastric Cancer ◽  
Cell Growth ◽  
Tumor Cell ◽  
Growth Suppression ◽  
Tumor Cell Growth ◽  
Annexin A10 ◽  
Cell Growth Suppression

Tumor Cell Growth Suppression by Chalcone (1,3-Diphenyl-2-Propen-l-One)

1997 ◽  
Vol 12 (1) ◽  
pp. 51-54 ◽  
Author(s):  
Hideo Kamei ◽  
Tatsurou Koide ◽  
Yoko Hashimoto ◽  
Takashi Kojima ◽  
Makoto Hasegawa
Keyword(s):  
Cell Growth ◽  
Tumor Cell ◽  
Growth Suppression ◽  
Tumor Cell Growth ◽  
Cell Growth Suppression

Tumor Cell Growth Suppression by Tannic Acid

1999 ◽  
Vol 14 (2) ◽  
pp. 135-138 ◽  
Author(s):  
Hideo Kamei ◽  
Tatsurou Koide ◽  
Yoko Hashimoto ◽  
Takashi Kojima ◽  
Makoto Hasegawa
Keyword(s):  
Cell Growth ◽  
Tumor Cell ◽  
Tannic Acid ◽  
Growth Suppression ◽  
Tumor Cell Growth ◽  
Cell Growth Suppression

scholarly journals Cell cycle genes as targets of retinoid induced ovarian tumor cell growth suppression

Oncogene ◽  
2001 ◽  
Vol 20 (55) ◽  
pp. 7935-7944 ◽  
Author(s):  
Dongmei Zhang ◽  
Scott Vuocolo ◽  
Valeria Masciullo ◽  
Teodoro Sava ◽  
Antonio Giordano ◽  
...  
Keyword(s):  
Cell Cycle ◽  
Cell Growth ◽  
Tumor Cell ◽  
Ovarian Tumor ◽  
Growth Suppression ◽  
Tumor Cell Growth ◽  
Cell Cycle Genes ◽  
Ovarian Tumor Cell ◽  
Cell Growth Suppression

scholarly journals Type I collagen aging impairs discoidin domain receptor 2-mediated tumor cell growth suppression

Oncotarget ◽  
2016 ◽  
Vol 7 (18) ◽  
pp. 24908-24927 ◽  
Author(s):  
Charles Saby ◽  
Emilie Buache ◽  
Sylvie Brassart-Pasco ◽  
Hassan El Btaouri ◽  
Marie-Pierre Courageot ◽  
...  
Keyword(s):  
Cell Growth ◽  
Tumor Cell ◽  
Type I Collagen ◽  
Growth Suppression ◽  
Type I ◽  
Tumor Cell Growth ◽  
Discoidin Domain Receptor ◽  
Discoidin Domain Receptor 2 ◽  
Cell Growth Suppression

scholarly journals Enhanced tumor cell growth suppression by an N-terminal truncated retinoblastoma protein.

1994 ◽  
Vol 91 (21) ◽  
pp. 9837-9841 ◽  
Author(s):  
H. J. Xu ◽  
K. Xu ◽  
Y. Zhou ◽  
J. Li ◽  
W. F. Benedict ◽  
...  
Keyword(s):  
Cell Growth ◽  
Tumor Cell ◽  
Retinoblastoma Protein ◽  
Growth Suppression ◽  
Tumor Cell Growth ◽  
Cell Growth Suppression

scholarly journals Analysis of wild-type and mutant p21WAF-1 gene activities.

1996 ◽  
Vol 16 (4) ◽  
pp. 1786-1793 ◽  
Author(s):  
J Lin ◽  
C Reichner ◽  
X Wu ◽  
A J Levine
Keyword(s):  
Amino Acid ◽  
Cell Growth ◽  
Tumor Cell ◽  
Cyclin D1 ◽  
Cyclin E ◽  
Growth Suppression ◽  
Nuclear Antigen ◽  
Tumor Cell Growth ◽  
Amino Acid Residues ◽  
Wild Type

The p21WAF-1 gene is positively regulated by the wild-type p53 protein. p21WAF-1 has been shown to interact with several cyclin-dependent kinase complexes and block the activity of G1 cyclin-dependent kinases (cdks). Mutational analysis with the p21WAF-1 gene localized a site, at amino acid residues 21 and 24 in the amino terminus of the protein, for p21WAF-1 binding to cyclins D and E. This region of the protein is conserved (residues 21 to 26) in other p21WAF-1 family members, p27kip-1 and p57kip-2. The same p21WAF-121,24 mutant also fails to bind to cyclin D1-cdk 4 or cyclin E-cdk 2 complexes in vitro, suggesting that amino acid residues 21 and 24 are important for p21WAF-1-cdk-cyclin trimeric complex interactions. The p21WAF-1 wild-type protein will suppress tumor cell growth in culture while p21WAF-1 mutant proteins with defects in residues 21 and 24 fail to suppress tumor cell growth. The overexpression of cyclin D or E in these cells will partially overcome the growth suppression of wild-type p21WAF-1 protein in cells. These results provide evidence that p21WAF-1 acts through cyclin D1-cdk4 and cyclin E-cdk2 complexes in vivo to induce the growth suppression. The p21WAF-1 binding sites for cyclins (residues 21 to 26), cdk2 (residues 49 to 71), and proliferating-cell nuclear antigen (residues 124 to 164) have all been mapped to discrete sites on the protein.

Curcumin micelles suppress gastric tumor cell growth by upregulating ROS generation, disrupting redox equilibrium and affecting mitochondrial bioenergetics

2020 ◽  
Vol 11 (5) ◽  
pp. 4146-4159 ◽  
Author(s):  
Xiaokun Lin ◽  
Lihua Wang ◽  
Liqian Zhao ◽  
Zheng Zhu ◽  
TongZuan Chen ◽  
...  
Keyword(s):  
Gastric Cancer ◽  
Cell Growth ◽  
Tumor Cell ◽  
Anticancer Activity ◽  
Gastric Tumor ◽  
Ros Generation ◽  
Mitochondrial Bioenergetics ◽  
Tumor Cell Growth ◽  
Redox Equilibrium

A proposed novel mechanism of anticancer activity of curcumin micelles through redox equilibrium in gastric cancer.

scholarly journals CircRNA_100269 is downregulated in gastric cancer and suppresses tumor cell growth by targeting miR-630

Aging ◽  
2017 ◽  
Vol 9 (6) ◽  
pp. 1585-1594 ◽  
Author(s):  
Yan Zhang ◽  
Hao Liu ◽  
Wende Li ◽  
Jiang Yu ◽  
Jin Li ◽  
...  
Keyword(s):  
Gastric Cancer ◽  
Cell Growth ◽  
Tumor Cell ◽  
Tumor Cell Growth

SRPK1 facilitates tumor cell growth via modulating the small nucleolar RNA expression in gastric cancer

2019 ◽  
Vol 234 (8) ◽  
pp. 13582-13591 ◽  
Author(s):  
Yandong Li ◽  
Shijun Yu ◽  
Xiao Wang ◽  
Xiaojuan Ye ◽  
Bin He ◽  
...  
Keyword(s):  
Gastric Cancer ◽  
Cell Growth ◽  
Tumor Cell ◽  
Rna Expression ◽  
Tumor Cell Growth ◽  
Small Nucleolar Rna ◽  
Nucleolar Rna
Sign in / Sign up

Export Citation Format

Share Document